ClearanceBrief
510(k) K091552 ยท KLW Masker, Tinnitus

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ApplicantAudifon GmbH & Co. KG, Debary FL, US
DecisionSubstantially Equivalent, Aug 12, 2009
ReceivedMay 27, 2009
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K091552

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.